Metabolic Associated Fatty Liver Disease in Patients With Chronic Glomerular Disease
The Association of Metabolic Associated Fatty Liver Disease in Patients With Chronic Glomerular Disease
1 other identifier
observational
500
0 countries
N/A
Brief Summary
The association of metabolic associated fatty liver disease in patients with chronic glomerular disease
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 14, 2024
CompletedFirst Posted
Study publicly available on registry
November 15, 2024
CompletedStudy Start
First participant enrolled
December 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2026
CompletedNovember 18, 2024
November 1, 2024
1 year
November 14, 2024
November 15, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
association between metabolic associated fatty liver disease and chronic kidney disease
To detect the association between metabolic associated fatty liver disease and chronic kidney disease with glomerular diseaese in Assuit university hospital.
through study completion, an average of 1 year
Study Arms (1)
study group
500 patients presented at Nephrology unit/Internal Medicine department (Assiut University Hospital) In the period 2024-2026.
Eligibility Criteria
All patients in this study will be subjected to 1. Detailed history and full clinical examination 2. Anthropometric measurements; Hight, weight, waist circumference. 3. Full lab investigations (Complete blood picture , kidney function tests, liver function tests, serum electrolytes, Ferritin, Uric acid level, Prothrombin time and concentration and serum albumin) 4. High sensitivity CRP 5. lipid profile (Fasting) 6. urine analysis, ACR. 7. Available documented renal biopsy 8. HBA1c 9. C- peptide levels. 10. FIB4 - score
You may qualify if:
- All CKD patient aging between (18-70) years with known tubule-glomerular diseases.
- At any eGFR.
- All CKD patient have either type I/II DM associated with CKD .
You may not qualify if:
- CKD patients of Unknown etiology.
- CKD patients with liver cirrhosis.
- CKD patients secondry to documented diabetic nephropathy.
- Patients with previous/current HBV or HCV.
- Pregnant CKD patients.
- Patient commencing any hepatotoxic medication.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- physician
Study Record Dates
First Submitted
November 14, 2024
First Posted
November 15, 2024
Study Start
December 1, 2024
Primary Completion
December 1, 2025
Study Completion
March 1, 2026
Last Updated
November 18, 2024
Record last verified: 2024-11